Pharmacogenetics Section, Department of Physiology and Pharmacology, Karolinska Institutet, SE-171 77 Stockholm, Sweden; email:
Pharmacoepigenetics Group, Department of Physiology and Pharmacology, Karolinska Institutet, SE-171 77 Stockholm, Sweden.
Annu Rev Pharmacol Toxicol. 2018 Jan 6;58:161-185. doi: 10.1146/annurev-pharmtox-010617-053021. Epub 2017 Oct 13.
Pharmacological treatment and exposure to xenobiotics can cause substantial changes in epigenetic signatures. The majority of these epigenetic changes, caused by the compounds in question, occur downstream of transcriptional activation mechanisms, whereby the epigenetic alterations can create a transcriptional memory and stably modulate cell function. The increasing understanding of epigenetic mechanisms and their importance in disease has prompted the development of therapeutic interventions that target epigenetic modulatory mechanisms, particularly in oncology where inhibitors of epigenetic-modifying proteins (epidrugs) have been successfully used in treatment, mostly in combination with standard-of-care chemotherapy, either provoking direct cytotoxicity or inhibiting resistance to anticancer drugs. In addition, emerging methods for detecting epigenetically modified DNA in bodily fluids may provide information about tumor phenotype or drug treatment success. However, it is important to note that many technical pitfalls, such as the nondeconvolution of methylcytosine and hydroxymethylcytosine, compromise epigenetic analyses and the interpretation of results. In this review, we provide an update on the field, with an emphasis on the novel therapeutic opportunities made possible by epidrugs.
药物治疗和接触外源化学物质会导致表观遗传特征发生重大变化。这些表观遗传变化大多数是由相关化合物引起的,发生在转录激活机制的下游,其中表观遗传改变可以产生转录记忆并稳定调节细胞功能。对表观遗传机制及其在疾病中的重要性的认识不断提高,促使人们开发针对表观遗传调节机制的治疗干预措施,特别是在肿瘤学领域,表观遗传修饰蛋白抑制剂(epidrugs)已成功用于治疗,主要与标准护理化疗联合使用,要么引起直接细胞毒性,要么抑制对抗癌药物的耐药性。此外,用于检测体液中表观遗传修饰 DNA 的新兴方法可能提供有关肿瘤表型或药物治疗成功的信息。然而,值得注意的是,许多技术陷阱,如甲基胞嘧啶和羟甲基胞嘧啶的非卷积,会影响表观遗传分析和结果的解释。在这篇综述中,我们提供了该领域的最新进展,重点介绍了 epidrugs 带来的新的治疗机会。